PR_b functionalized stealth liposomes for targeted delivery to metastatic colon cancer

被引:17
作者
Adil, Maroof [1 ]
Belur, Lalitha [2 ]
Pearce, Timothy R. [3 ]
Levine, Rachel M. [1 ]
Tisdale, Alison W. [1 ]
Sorenson, Brent S. [4 ]
Mclvor, R. Scott [2 ]
Kokkoli, Efrosini [1 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Diagnost & Biol Sci, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
FIBRONECTIN-MIMETIC PEPTIDE; GENE DELIVERY; IN-VIVO; PEGYLATED LIPOSOMES; DNA COMPLEXES; ALPHA-5-BETA-1; INTEGRIN; ANTITUMOR EFFICACY; PROTON SPONGE; CELL-CYCLE; POLYETHYLENIMINE;
D O I
10.1039/c2bm00128d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A gene delivery system was designed to carry a payload to integrin overexpressing cells. Branched-polyethyleneimine (bPEI) condensed plasmid DNA was encapsulated into targeted stealth liposomes, thereby combining the condensing and transfection properties of bPEI with the stealth and targeting properties of the liposomal carrier system. PR_b was used as a targeting ligand - a peptide we designed to bind specifically to the cancer cell surface marker alpha(5)beta(1) integrin - and such a robust receptor-ligand interaction achieved higher specificity than what has been previously reported for targeted delivery systems. In the process of formulating the PR_b functionalized gene delivery vehicle, we developed a protocol to fully encapsulate condensed DNA in liposomes and accurately quantify the total DNA in the system. We demonstrate that compared to non-targeted stealth liposomes and non-encapsulated condensed DNA, the PR_b functionalized stealth liposomes mediated improved in vitro transfection specifically to colon cancer cells overexpressing the alpha(5)beta(1) integrin. Furthermore, when administered in vivo to metastatic tumor bearing mice, PR_b functionalized stealth liposomes outperformed non-targeted liposomes and delivered genes specifically to the tumor site.
引用
收藏
页码:393 / 401
页数:9
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